M11: Face And Neck Flashcards

1
Q

When does development of the face occur, when is it complete

A

5 wks LMP

10 wks

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2
Q

What does the face develop from

A

5 main facial processes that move together and fuse:

1 frontonasal process
2 maxillary prominences
2 mandibular prominences

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3
Q

How does the frontonasal process of the face develop

What does it form

A

Starts superior and move inferiorly

Mid forehead, nose, central upper lip, central maxilla and anterior palate

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4
Q

Another name for anterior palate

A

Primary palate

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5
Q

How does the maxillary and mandibular prominences of the face develop

What do they form

A

Maxillary moves medially And fuse to form:

Cheeks
Lateral upper lip
Maxilla
Secondary palate

Mandible fuse to form the mandible

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6
Q

Another name for Secondary palate

A

Posterior palate

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7
Q

Describe the migration of the nose where does it start

A

Starts above the orbits as 2 widely spread nasal placodes that move medially and inferiorly

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8
Q

Define placodes

A

Areas of ectoderm tissues that form the sense organs

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9
Q

Describe the migration of the eyes

Where do they start

A

Start laterally and move medially

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10
Q

Describe the migration of the ears

Where do they start

A

Below the mandible and move laterally and upwards

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11
Q

Are facial anomalies common

What do they often cause

A

Yes

Polyhydramnios

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12
Q

facial anomalies are associated w/ what other anomalies

A

Other non-facial anomalies due to chromosomal abnorm.

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13
Q

What drugs/teratogens can affect the development of the face

A

Alcohol
Codeine
Valium
Anti-epileptics

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14
Q

Which chromo abnorm is commonly associated w facial anomalies

A

T13, then T18

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15
Q

What view do we assess the orbital distance, the lens and binocular distance

A

Axial view/BPD with the orbits and cranium in view

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16
Q

Which view is used to assess the nose/lips

What are we assessing for

A

Tangential coronal… important to have the soft tissues, not the bone

Intact upper lip
Presence of 2 nostrils

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17
Q

What do we asses for when scanning the profile

A

Prominence of chin and forehead
Protruding tongue or flattened nose
Assess for nasal bone

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18
Q

How should the alignment of the bones appear in the profile image

What about the forehead

A

Maxilla, nasal bone, chin

Forehead shouldn’t extend out to the same level of the other bones

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19
Q

When assessing the profile, how should the chin be positioned

A

Off the chest

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20
Q

Propose of 3D imaging

A

Give parents and surgeons an idea of what to expect at birth

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21
Q

How far apart should the orbits be

A

Separated by a distance of 1 orbit

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22
Q

Which measurement for the orbits can be used to date preg when BPD cant be obtained

A

Outer orbital distance

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23
Q

Describe anophthalmia

A

Congenital absence or severe hypoplasia or the eyes

LOOK FOR LENS

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24
Q

anophthalmia is associated w/ which chromo abnorm

A

T13

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25
Q

Describe micophthalmia

Which measurement is important

A

Small eyes

Interocular measurement

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26
Q

micophthalmia is associated w/ which chromo abnorm

A

T13

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27
Q

Describe hypertelorism

What commonly causes it
Other causes

A

Widely spread eyes

Mass blocking anterior migration of the eyes
Craniosynostoses , eyes cant migrate

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28
Q

Describe hypotelorism

Which measurement if important

Associated w/ which chromo abnorm

A

Eyes close together

Binocular measurement

T13

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29
Q

Describe cyclopia

Associated w/ which abnorm of the nose

Asssociated w/ which chromo abnorm

A

Fusion of eyes into one orbit

supraorbital proboscis

T13

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30
Q

Describe ethmocephaly

A

2 closely spaced but separate eyes w/ a supraorbital proboscis

31
Q

Describe cebocephaly

A

2 closely spaced but separate eyes w/ a centrally placed nose w/ only one blind ended nostril

32
Q

What is a proboscis

A

Tuft of tissue, usually above the eyes… no normal nose

33
Q

5 patterns of cleft lip and palate

more cases are what type

A
isolated cleft lip
unilateral cleft lip and palate
bilateral cleft lip and palate
midline cleft lip and palate
facial defects associate w/ amniotic bands

cleft lip and palate together

34
Q

is US better at detecting cleft lip or palate

A

lip, palate is hard to see on US and often missed

35
Q

which type of cleft lip is more likely to be associated w/ additional anomalies

A

isolated cleft lip

36
Q

2 abnormalities often seen w/ clefting

A

polyhydramnios and sm stomach b/w the defect can disturb swallowing

37
Q

cleft lip should not be confused w/ which normal anatomy

38
Q

lateral cleft lip is associated w/ which chromo abnormality

39
Q

US appearance of bilateral cleft lip

A

snout like appearance b/c upper lip isn’t attached on either side on the mouth so ‘floats’ in the amniotic fluid

40
Q

median cleft face has a stronger association w/ which chromo abnorm

41
Q

describe median cleft face

which structures didn’t fuse to cause this

A

cleft in the middle of the nose and including the nose (missing the septum)

nasal and maxillary structures failed to fuse

42
Q

best view to assess for cleft palate

look around which area in the mouth?

A

TRX

around tooth buds

43
Q

cleft palate can be mistaken for which normal facial structures

A

oral cavity or ethmoid sinuses

44
Q

describe macroglossia

associate w/ which chromo abnorm

A

abnormally large protruding tongue beyond the lips

T21 and beckwith-wiedemann syndrome

45
Q

abnormalities seen w/ beckwith-wiedemann syndrome

A
macroglossia
macrosomia (big baby)
omphalocele
renal hyperplasia or dysplasia
increased risk of wilms tumor and hepatoblastoma
46
Q

define micrognathia

retrognathia

A

small chin

receding chin

47
Q

what is frontal bossing

associated w/ what anomalies

A

protruding forehead

skeletal dysplasia

48
Q

low set and/or small ears are associated w/ which abnormalities

A

T21, 18 or 13

49
Q

when does the thyroid start to function

what abnormalities can occur

A

12 wks

hyper or hypothyroidism

50
Q

maternal causes of hyperthyroidism in the fetus

A

maternal graves disease

51
Q

Us appearance of hyper or hypothyroidism

A
  • thyroid would be enlarged, neck mass is seen that may cause the fetal neck to be hyperextended
  • polyhydramnios due to obstruction
52
Q

what can fetal thyroid dysfunction lead to

treatment

A

IUGR
oligohydramnios
tachycardia

thyroid medicaltion administered to mom

53
Q

what is a nuchal cord

A

umbilical cord wrapped 2 or more times around the neck…

more likely to be a poor prognosis if the cord it wrapped multiple times and tightly… loose wrapping or 1 loop is insignificant

54
Q

best plane to assess nuchal cord

55
Q

describe cystic hygroma

prognosis

A

separated nuchal fluid located posterior and lateral to the neck… usually multiocular lymph fluid lined by lymphatic endothelium

poor

56
Q

how does a cystic hygroma arise

A

thought to arise due to a failure of the lymphatic sys to develop a communication to the venous sys of the neck…. so lymph can’t drain properly.

57
Q

are all cystic hygromas lymphatic in origin

58
Q

cystic hygroma associations

A
hydrops
chromo abnormalities (>60%)
cardiac abnormalities
fetal alcohol syndrome
can be seen after IUD
59
Q

cystic hygroma is associated w/ which chromo and genetic abnorm

A

turners
T21
noonan syndrome

60
Q

US appearance of cystic hygroma

when can they be seen

A

hypo fluid w/ random septations

as early as 10 wks

61
Q

cystic hygroma can be mistaken of which normal anatomy

A

nuchal translucency

62
Q

Ddx for cystic hygroma

A

poster encephalocele, but brain, skull, spine are all normal w/ cystic hygroma

63
Q

when is the nuchal translucency seen
how big is the CRL at this time

normal value

A

11-13 wks and 6d gestation
45-84 mm

< 3mm but depends on maternal age

64
Q

increased size of nuchal T associated w/ abnormalities

A

chromosomal and other abnormalities

65
Q

how do you measure a NT

A
zoom, only head and fetal chest on the screen
perfect midline sag
neutral spinal/chin position
decrease compression
measure on to on
66
Q

when is the nuchal fold (NF) assessed

what causes it to be thick

A

16-24 wks for T21

subcutaneous edema

67
Q

when do we stop measuring nuchal fold

A

24 weeks, after this babies have different growth curves so could be larger but norm

68
Q

what positioning can help visualize the NF better

A

tip posterior of babies head anteriorly

69
Q

what are teratomas composed of

can they obstruct swelling

A

3 germ cell layers

yes

70
Q

what is dystocia? what can cause it

A

difficult labor/birth

teratoma

71
Q

what affects can a teratoma have after birth

A

compromised breathing and swallowing

72
Q

US appearance of teratoma

A

solid mass, hyperextension of the fetal neck if the mass is big

73
Q

With hypertelorism, which eye measurements are normal and which are abnormal

A

N: OOD
AB: IOD